Canonical Allele Identifier: CA154827737
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs895497946

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293295T>C , CM000669.2:g.17293295T>C GRCh38
NC_000007.13:g.17332919T>C , CM000669.1:g.17332919T>C GRCh37
NC_000007.12:g.17299444T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-3002T>C ENSP00000495987.1:n.-202-3002T>C
XR_927069.1:n.293+1871A>G
XR_927070.1:n.293+1871A>G
XR_927071.1:n.293+1871A>G
XR_927072.1:n.294+1871A>G
XR_927073.1:n.295+1871A>G
XR_927073.2:n.295+1871A>G